Nov 29, 2022

Synscoby Co Culture

Day 0 (Wednesday PM) November 30th

  1. Inoculate K. rhaeticus from glycerol stock in 5mL YPD + 1% cellulase
  2. Place in shaking incubator at 30˚, 250rpm for 3 days
  3. Streak S. cerevisae on YPD plates so fresh when inoculating on day 3.

To avoid contamination the YPD + Cellulase 1% were added into a centrifuge tube in the hood, then added to smaller to tubes with snap off caps.

Cellulase                                                    YPD


Outside of the hood we added the K.Rhaeticus with tooth picks into 30 ml tubes.

There were a total of 6 tubes so we can start co coulture of (3x BY4741p + 3 x Venus Ura)









Streaking new fresh yeast from the October batch into Agar plates 


Isolating yeast at this point is as simple as taking a very small amount of your culture and rubbing (streaking) it on to an agar plate. Because of the stable, non-liquid agar medium, once streaked, single colonies of microbes are essentially stranded by themselves.

After a few days or weeks (depending on incubation temperature and microbe population), they’ll multiply and grow large enough to be seen with the naked eye. At that point, it’s a matter of selecting the colonies you like and growing them up to larger amounts.

It’s impossible to stress enough how important cleanliness and sanitation are at this point in the process. If you truly want a pure strain, you need to ensure you’re not contaminating what you’re trying to isolate with other cultures.










Day 2 (Friday PM) December 2nd

  1. Inoculate S. cerevisiae from plate in 5mL YPD
  2. Place in shaking incubator at 30˚, 250rpm for 1 day



Day 3 (Saturday) December 3rd

  1. Centrifuge K. rhaeticus at 3,220 g  (5119 rpm) for 10 minutes. 
  2. Resuspend K. rhaeticus cells in YPS to OD600=2.5. This helps to remove cellulase.
  3. Dilute S. cerevisiae in YPS to OD600 = 0.01
  4. Combine K. rhaeticus and S. cerevisiae in 50mm petri dish, inoculating K. rhaeticus 1/50 and S. cerevisiae 1/100 in fresh YPS-optiprep. Final volume should be 15mL.
  5. Incubate at 30˚ for 3 days under static conditions. Do not move co-cultures while growing or BC layers will come apart.




*****


YPS

  • 5g yeast extract

  • 10g peptone

  • 10g sucrose


HS Recipe x 500 ml

  • 2.5g yeast extract

  • 2.5g peptone

  • 1.35g sodium phosphate

  • 0.75g citric acid

  • 10g sucrose

  • 500ml distilled water

**Snap off cap works best for K. Rhaeticus growth 

Dextrose instead of sugar

  The pellicle grew nicely BUT the dextrose measurement * might not be the same as the sugar*  measurement.  Given that the structure is dif...